EP0346834A2 - Procédé de préparation de polymères - Google Patents

Procédé de préparation de polymères Download PDF

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Publication number
EP0346834A2
EP0346834A2 EP89110694A EP89110694A EP0346834A2 EP 0346834 A2 EP0346834 A2 EP 0346834A2 EP 89110694 A EP89110694 A EP 89110694A EP 89110694 A EP89110694 A EP 89110694A EP 0346834 A2 EP0346834 A2 EP 0346834A2
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Prior art keywords
cosolvent
water
polymer
monomer
hydrophobic
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EP0346834A3 (fr
EP0346834B1 (fr
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Peter Graham Montague
Peter Bainbridge
Philip Ashley Lagar
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National Starch and Chemical Investment Holding Corp
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National Starch and Chemical Investment Holding Corp
National Starch and Chemical Corp
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00—Processes of polymerisation
    • C08F2/12—Polymerisation in non-solvents
    • C08F2/16—Aqueous medium

Definitions

  • This invention relates to a process for the preparation of polymeric compositions comprising at least one hydrophilic monomeric component and at least one hydrophobic monomeric component.
  • Polymers of this class are especially adapted for use in detergent compositions.
  • Polymers containing both hydrophilic and hydrophobic moieties are useful in a wide variety of applications.
  • preparation of these polymers is often difficult, inefficient, and not cost effective, particularly when it is desired to prepare the polymer in relatively high solids, low viscosity, essentially aqueous form.
  • Preparation of these polymers have frequently been described in the prior art.
  • GB 1,052,924 discusses the polymerization of methacrylic acid with stearyl or lauryl methacrylate in a wide range of non-aqueous solvents. This method suffers from the fact that the solvents are toxic and expensive and the final form of the polymer is inconvenient to use due to the presence of these solvents.
  • Buscall and Corner in EP 99179 describe the preparation of these copolymers in pure cosolvent, and subsequent work-up of the preparation to provide aqueous solutions of distillation and total solvent exchange.
  • this procedure is followed, starting from an aqueous cosolvent mixture where the water content is in a ratio of 1.5:65 parts of water: acetone.
  • Hydrophobic acrylonitrile emulsions are produced in GB 1,351,304, in a form of non-aggregated particles, in a medium of dimethyl sulphoxide and water.
  • the ratio of dimethyl sulphoxide to water is from 85:15 to 60:40, i.e. where the cosolvent is in excess to water.
  • GB 215,565 teaches preparation of copolymers of acrylic acid and various hydrophobic ethoxylated monomers in a mixture of isopropanol and water, where the ratio of water to isopropanol is 125:240.
  • the polymer in addition to using cosolvent in excess, can be produced in a limpid (clear) solution form, and this of necessity, will have a high viscosity at relatively low solids.
  • GB 498,383 prepares copolymers of vinyl alkyl ketones in aqueous monohydric alcohols.
  • the solvent preparations are claimed to vary within wide limits, the exemplified polymers are prepared where the cosolvent is present in an amount of at least 60%. No examples are described where the water present is in excess or where the polymers are not in a limpid (clear) state.
  • An alternative method is to use an emulsifier to disperse the hydrophobic monomer and to subsequently obtain a copolymer having a uniform composition.
  • the need for emulsifiers increases the cost of the polymerization process and may have a deleterious effect on the properties of the final polymer.
  • EP 57,875 teaches polymerization of the hydrophobic and hydrophilic species in an aqueous medium containing an emulsifier for the hydrophobic monomer. This is exemplified by sodium dodecyl sulphate, and is essential for the preparation of homogeneous stable copolymers.
  • Cosolvent can be omitted altogether, when the hydrophobic moieties are more hydrophilic, by the inclusion of ethoxylate surfactant coponents in the monomers.
  • polymers of surfactant type monomers having pendent hydrophobic portions are polymerized with water soluble monomers, preferably acrylic acid, to give copolymers useful in detergent compositions.
  • a preferred method is copolymerization in aqueous solution although precipitation and suspension polymerization is described.
  • hydrophilic/hydrophobic polymers can be efficiently prepared using conventional aqueous polymerization procedures, but employing a process wherein the polymerization is carried out in the presence of a suitable cosolvent and wherein the amount of cosolvent is carefully monitored so as to maintain the ratio of water to cosolvent equal or greater than unity during the reaction, thereby keeping the polymer as it forms in a sufficiently mobile condition and preventing unwanted homopolymerization and precipitation of the polymer from the hydrophobic monomer.
  • the process of the invention provides a product in a unique form as a relatively high solids, low viscosity, opaque or semi-­opaque product intermediate between a true clear or limpid solution, and an emulsion consisting entirely of non-agglomerated particles.
  • the product exhibits no gelling, coagulation or product separation on standing for at least two weeks. It is further characterized in that upon dilution to 0.25% solids content W/W, the turbidity of the resultant preparation is at least 10 Nephelometric Turbidity Units (N.T.U.'s).
  • Water soluble monomers suitably employed to form the hydrophilic backbone include those which are sufficiently water soluble to form at least a one weight percent solution when dissolved in water and readily undergo polymerization to form polymers which are water soluble at ambient temperature and at a pH of 3.0 to 12.5, preferably more than 1 gram per liter, more preferred more than 5 grams per liter, most preferred more than 10 grams per liter.
  • Exemplary water soluble monomers include ethylenically unsaturated amides such as acrylamide, methacrylamide and fumaramide and their N-substituted derivatives such as 2-acrylamido-2-methylpropane sulfonic acid, N-(dimethylaminomethyl) acrylamide as well as N-­(trimethylammoniummethyl) acrylamide chloride and N-­(trimethylammoniumpropyl)methacrylamide) chloride; ethylenically unsaturated carboxylic acids or dicarboxylic acids such as acrylic acid, maleic acid, methacrylic acid, itaconic acid, fumaric acid, crotonic acid, aconitic acid and citraconic acid; and other ethylenically unsaturated quaternary ammonium compounds such as vinylbenzyl trimethyl ammonium chloride; sulfoalkyl esters of unsaturated carboxylic acids such as 2-sulfoethyl methacrylate;
  • the hydrophilic backbone may contain small amounts of relatively hydrophobic units, e.g., those derived from polymers having a solubility of less than 1 g/l in water, provided that the overall solubility of the hydrophilic polymer backbone still satisfies the solubility requirements as specified here above.
  • relatively water insoluble polymers are polyvinyl acetate, polymethyl methacrylate, polyethyl acrylate, polyethylene, polypropylen, polystyrene, polybutylene oxide, polypropylene oxide, polyhydroxypropyl acrylate.
  • Suitable hydrophobic monomers generally include those which are (1) water-insoluble, i.e., less than 0.2 weight part of the hydrophobic monomer will dissolve in 100 weight parts water and (2) ethylenically unsaturated compounds having hydrophobic moieties.
  • the hydrophobic moieties (when isolated from their polymerizable linkage) are relatively water insoluble, preferably less than 1 g/l, more preferred less than 0.5 g/l, most preferred less than 0.1 g/l at ambient temperature and a pH of 3.0 to 12.5.
  • the hydrophobic moieties preferably have at least 5 carbon atoms and are most preferably pendant organic groups having hydrophobicities comparable to one of the following: aliphatic hydrocarbon groups having at least five carbons such as C5 to C50 alkyls and cycloalkyls; polynuclear aromatic hydrocarbon groups such as napthyls; alkylaryls wherein the alkyl group has one or more carbons; haloalkyls of 5 or more carbons, preferably perfluoralkyls; polyalkylenoxy groups wherein alkylene is propylene or high alkylene and there is at least one alkyleneoxy unit per hydrophobic moiety; and siloxane moieties.
  • Exemplary hydrophobic monomers include the higher alkyl esters of alpha, beta ethylenically unsaturated carboxylic acids such as dodecyl acrylate, dodecyl methacrylate, tridecyl acrylate, tridecyl methacrylate, tetradecylacrylate, tetradecylmethacrylate, octadecyl acrylate, octadecyl methacrylate, octyl half ester of maleic anhydride, dioctyl diethyl maleate, and other alkyl esters and half esters derived from the reactions of alkanols having from 5 to 50 carbon atoms with ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic anhydride, fumaric acid, itaconic acid and aconitic acid; alkylaryl esters of ethylenically unsaturated carboxylic acids
  • the hydrophobic monomer may be used singly or mixtures thereof may be employed.
  • the ratio of hydrophilic to hydrophobic monomers may vary from about 100:1 to 5:1.
  • the molecular weight average weights (Mw.) of the resultant polymers varying from 500 to 100,000 or above when measured by gel permeation chromotography using a polyacrylate standard.
  • GPC Gel permeation chromatography
  • the approximate true molecular weight of the sample can be calculated, but if such standards are not available, it is common practice to use some other well characterized standards as a reference.
  • the molecular weight obtained by such means is not the absolute value, but is useful for comparative purposes. Sometimes it will be less than that resulting from a theoretical calculation for a dimer.
  • the process of the present invention is particularly suitable for the preparation of deflocculating polymers disclosed in co-pending application filed of even dated herewith.
  • the process of the invention is especially useful for preparation of polymers of the general formula: wherein z is 1; (x + y): z is from 5: 1 to 100: 1; in which the monomer units may be in random order; y being from 0 up to a maximum equal to the value of x; and n is at least 1;
  • R1 represents -CO-O, -O-, -O-CO-, -CH2-, -CO-NH- or is absent;
  • R2 represents from 1 to 50 independently selected alkyleneoxy groups, preferably ethylene oxide or propylene oxide groups, or is absent, provided that when R3 is absent and R4 represents hydrogen, then R2 must contain an alkyleneoxy group with at least 3 carbon atoms;
  • R3 represents a phenylene linkage, or is absent;
  • R4 represents hydrogen or a C5 ⁇ 24
  • Another class of polymers produced in accordance with the present invention comprise those of formula II: wherein: Q2 is a molecular entity of formula IIa: wherein z and R1 ⁇ 6 are as defined for formula (I); A1 ⁇ 4 are as defined for formula (I);
  • Q1 is a multifunctional monomer, allowing the branching of the polymer, wherein the monomers of the polymer may be connected to Q1 in any direction, in any order, therewith possibly resulting in a branched polymer.
  • Q1 is trimethyl propane triacrylate (TMPTA), methylene bisacrylamide or divinyl glycol.
  • n and z are as defined above; v is 1; and (x + y + p + q + r): z is from 5: 1 to 100: 1; in which the monomer units may be in random order; and preferably either p and q are zero, or r is zero; R7 and R8 represents -CH3 or -H; R9 and R10 represent substituent groups such as amino, amine, amide, sulphonate, sulphate, phosphonate, phosphate, hydroxy, carboxyl and oxide groups, or ( C2H4O) t H, wherein t is from 1-50, and wherein the monomer units may be in random order.
  • they are selected from -SO3Na, - CO-O-C2H4, -OSO3Na, -CO-NH-C(CH3)2CH2SO3Na, -CO-NH2, -O-CO-CH3, -OH.
  • polymers of formulae I and II are in the form of a salt
  • some polymers will be full salts (A1 -A4 all other than hydrogen)
  • the salts of the polymers of formulae I and II may be formed with any organic or inorganic cation defined for A1 -A4 and which is capable of forming a water-soluble salt with a low molecular weight carboxylic acid.
  • Preferred are the alkali metal salts, especially of sodium or potassium.
  • Another class of polymers produced in accordance with the present invention comprise those of formula III.
  • Q3 is derived from a monomeric unit IIIa comprising Q4 is derived from the molecular entity IIIb and Q5 is derived from a monomeric unit IIIc
  • R1 - R6 are defined as in formula I, (a+b+c):
  • Q4 is from 5:1 to 100:1, in which the monomer units may be in random order, a, b, c, d, e, f, g, h may be an integer of zero, n is at least 1;
  • B1, B2, B3, B4 are organic or inorganic anions;
  • w is zero to 4;
  • R11 is independently selected from hydrogen or C1-C4 alkyl; and R12 is independently selected from C5 to C24 alkyl or alkenyl, aryl cycloalkyl, hydroxyalkyl, or alkoxyalkyl
  • the anions represented by B1, B2, B3, B4 are exemplified by the halide ions, sulphate sulphonate, phosphate, hydroxide, borate, cyanide, carbonate, bicarbonate, thiocyanate, isocyanate, sulphide, cyanate, acetate and the other common inorganic and organic ions.
  • Preferred anions are chloride and sulphate.
  • a weight average molecular weight in the region to from 500 to 500,000, most preferably from 1000 to 30,000, especially from 2000 to 10,000 when measured by GPC using polyacrylate standards.
  • the molecular weights of the standards are measured by the absolute intrinsic viscosity method described by Noda, Tsoge and Nagasawa in Journal of Physical Chemistry, Volume 74, (1970), pages 710-­719.
  • a measure of molecular weight can be made by measuring a standard viscosity (S.V.), determined at 15.0% solids, 23°C in a 1.0 molar sodium chloride solution using a Brookfield Synchro-lectric® viscometer, Model LVT with a LCP adaptor, at a speed of 60 RPM. It is preferred to have a polymer with a S.V. from 1 to 100 cps., more preferably from 2-50 cps., most preferably 3-25 cps.
  • cosolvent chosen for the reaction will vary depending upon the particular monomers to be polymerized.
  • the cosolvent selected should be miscible with water, dissolve at least one of the monomers, but not react with the monomers or with the polymer as it is produced and be substantially readily removed by simple distillation or azeotropic distillation procedures.
  • Suitable cosolvents include, but are not limited to lower (C1 to C4) alcohols, acetone, esters, and ketones. Isopropanol and n-propanol are the most preferred.
  • the ratio of water to cosolvent must be carefully regulated. If too low an amount of cosolvent is employed, precipitation of hydrophobic monomer or homopolymer may occur, too high a cosolvent level is more expensive and time consuming to remove; results in too high viscosity product and, in some cases, may cause precipitation of the water soluble polymer. It will be apparent to one skilled in the art that the precise ratio of water to cosolvent will vary depending upon the specific hydrophilic and hydrophobic monomers employed as well as the amounts thereof; the particular cosolvent chosen and the desired molecular weight of the final polymer.
  • the polymerization is carried out in the presence of free-radical initiators.
  • free-radical initiators examples of water-soluble free-radical initiators which are suitable for the polymerization are the usual thermal decomposition initiators such as hydrogen peroxide, peroxydisulfates, especially sodium peroxydisulfate or ammonium peroxydisulfate, or 2,2′azobis(2-amidinopropane) hydrochloride.
  • Redox initiators such as tertiary butyl hydroperoxide/bisulphite tertiary butyl hydroperoxide/sodium formaldehyde sulphoxylate; or hydrogen peroxide with a ferrous compound can also be used.
  • the polymerization takes place in an aqueous cosolvent medium, and the concentration is advantageously chosen so that the aqueous cosolvent solution contains from 10 to 55%, preferably from 20 to 40% by weight of total monomers.
  • the reaction temperature can vary within wide limits, but is advantageously chosen to be from 60° to 150°C, preferably from 70° to 95°C. If the reaction is carried out at above the boiling point of water, a pressure-tight vessel, such as an autoclave, is chosen as the reaction vessel.
  • regulators conventionally used for free-radical polymerization in an aqueous medium e.g. thioglycolic acid or C1 to C4 aldehydes, or chain lengtheners, such as methylene bisacrylamide or divinyl glycol
  • chain lengtheners such as methylene bisacrylamide or divinyl glycol
  • the turbidity of the prepared polymers was measured using a Hach Model 2100A Turbidimeter. It was found that direct measurement on the polymers was not possible, and that useful readings could only be made when the polymers were diluted to 0.25% solids content W/W with deionized water. Measurements were made at ambient temperatures and no further adjustments were made to the diluted sample. The turbidity was read from the scale as Nephelometric Turbidity Units (N.T. U.'s)
  • a monomer mixture was prepared consisting of a hydrophilic monomer acrylic acid 216g, (3.0 moles) and a hydrophobic monomer, Methacrylester 13, a methacrylic ester with average chain length of 13 carbons available from Rohm, 32g (0.12 moles). This gave a molar ratio of hydrophilic to hydrophobic monomer of 25:1.
  • the monomer mixture was pumped into the reaction vessel over a period of about 3 hours keeping the reaction mass at 80-85°C, and simultaneously introducing, over a period of 4 hours, by pumping in an independent stream, an initiator solution consisting of a 100 g of 4% aqueous solution of sodium persulphate.
  • the ratio of water and cosolvent to polymer had risen to 2.82:1 and the water to isopropanol ratio to 2.5:1.
  • the reaction contents were held at 80-85°C for a period of about one further hour, giving a total time from the start of the monomer and initiator additions of about 5 hours.
  • the isopropanol was then substantially removed from the reaction product by azeotropic distillation under vacuum, until the residual isopropanol content was less than 1% as measured by direct gas liquid chromatography using a flame ionization detector.
  • the polymer was neutralized to approximately pH7 by adding, at 40°C and below, 230 grams (2.76 moles) of 48% caustic soda solution with water added back as necessary to bring the solids to approximately 35%.
  • the product was an opaque viscous product, having a solids content of approximately 35% and a viscosity of 1500 cps at 23°C as measured by a Brookfield Synchro-Lectric® viscometer model RVT, spindle 4, at 20 rpm.
  • the molecular weight distribution of the polymer produced was measured by aqueous gel permeation chromatography, using an ultra violet detector set at 215 nm.
  • the number average (Mn) and weight average (Mw) molecular weights were measured from the chromatogram so produced, using fractionated sodium polyacrylate standards to construct a calibration graph.
  • the molecular weight of these standards had been measured by the absolute intrinsic viscosity method described by Noda, Tsuge and Nagasawa in the Journal of Physical Chemistry, Vol. 74 (1970), pages 710 to 719.
  • the polymer produced had a Mn of 1600 and Mw of 4300.
  • the pH of the product was 7.0 and an 0.25% solution of the product had a turbidity of 110 N.T.U's.
  • Table I Water: Isopropanol Ratio Polymer Produced Sample Start of Reaction End of Reaction Mn Mw pH % Solids Visc. cps Turbidity (0.25%, N.T.U.'s) I 2.0 2.5 1600 4300 7.0 35.6 1500 110 IIA 2.0 6.0 - - - - - 400 IIB 3.0 3.7 1800 5400 6.5 34.9 300 500 IIC 1.4 1.8 1350 3500 7.8 35.0 9000 10 IID 1.0 1.3 1000 2900 7.4 34.0 35000 1.8
  • Example IIA In contrast to the copolymer of Example I which exhibits an optimum balance of high solids and low viscosity, the cosolvent ratios used in Example IIA gave a severely coagulated product with a large amount of sticky coagulum coating the reactor walls and stirrer.
  • the ratio used in Example IIB is the maximum water isopropanol ratio useful in producing this specific copolymer since the resultant product was an opaque, thin liquid containing a small amount (about 5%) of coagulum.
  • the ratio of water to isopropanol was reduced in Example IIC, the product became thicker but remained semi-opaque and homogeneous, while the ratio in Example IID gave a practically clear, homogeneous extremely thick product which had to be diluted prior to application.
  • Example IID required dilution to 26.7% solids in order to achieve a viscosity of 1100 cps, similar to that of Example I. This gives an advantage of about 9% in solids content of Example I over Example II, and is important economically for reactor throughput of product during manufacture, transportation, storage and lack of dilution before use.
  • the water to isopropanol ratio should be within the range of 1.4 to 3.7 during the reaction.
  • the turbidity of an 0.25% solution of the polymer should be 10 N.T.U.'s or greater. (Note there is a little decrease in molecular weight as the water to isopropanol ratio is lowered, however the viscosity is unexpectedly seen to rise.)
  • Example II Sample Ratio acrylic acid to methacrylate ester (molar) Water - Cosolvent Ratio pH Solids Viscosity cps Mw Mn Turbidity (0.25%, NTU) Start End IIIA (1) 50 2.3 2.6 5.1 21.5% 5200 15000 3700 53 IIIB (1) 50 2.0 2.5 4.5 32.4% 4000 7500 3600 12 IIIC (3) 25 infinity infinity - - - - - IIID (2) 25 2.0 2.5 6.8 33.9% 1000 7200 3000 310 IIIE (1) 25 2.3 2.6 3.8 18.5% 1500 32000 4700 210 IIIF (2) 12 2.0 2.5 7.6 39.3% 1200 3800 1500 250 IIIG (1) 6 2.0 2.4 4.5 12.8% 9000 27000 7200 950 (1) Normal propanol was used as cosolvent. (2) Isopropanol was used as cosolvent. (3) No
  • Sample IIIC which did not utilize any cosolvent resulted in a product which was not homogeneous, and which precipitated. All other polymers were opaque liquids which were homogeneous and did not separate on standing for at least two weeks.
  • copolymers as described above may be prepared with isopropanol or normal propanol using the procedure of the present invention and varying the hydrophilic to hydrophobic monomer ratio within the range of about 6:1 to 50:1; Mw within the range of about 3800 to 32,000; viscosity ranges of 1000 to 9000 cps at desirable high solids levels, and an 0.25% turbidity greater than 10 N.T.U's.
  • the above-described copolymers were readily produced using a water to cosolvent ratio in the range of about 2.0 to 2.6 during the reaction. Based on the properties observed in these polymers as well as the results obtained in Examples I and II, it is contemplated that similar satisfactory results could be obtained using water to cosolvent ratios of about 1.4 to 3.7 during the reaction.
  • This example illustrates the use of another hydrophobic monomer, Sipomer LMA® a lauryl methacrylate ester available from Alcolac, and the scale-up to larger size equipment.
  • Example I The procedure of Example I was repeated using an initial monomer charge of 1095 g (15.21 moles) acrylic acid and 155 g (0.605 mole) lauryl methacrylate.
  • the final water; isopropanol ratio was 1.92:1.
  • Example II The procedure of Example I was repeated using the raw materials and amounts shown in Table III. In all cases, acrylic acid was used in a molar ratio of 25:1 acrylic acid to hydrophobic monomer with neutralization, if performed, to the pH values indicated.
  • Initiator systems are identified as follows: (A) 100 g of 1% sodium persulphate and (B) 100 g of 4% sodium persulphate.
  • a sample of mono octadecyl (monostearyl) maleate was prepared in a similar manner, but using 405 g octadecanol (1.5 moles) and 147 g maleic anhydride (1.5 moles).
  • the isopropanol was removed by azeotropic distillation until a level of less than 1% was obtained as measured by direct injection gas chromatography, and the product neutralized to approximate neutrality by adding 416 g of 48% caustic soda solution (5.0 moles).
  • the product was semi-opaque, solids content 41.4%, pH 7.5; Mn 1200; Mw 3000; Vicosity 1800 cps (spindle 4 speed 20), and had an 0.25% turbidity of 12 N.T.U's.
  • Example VI The procedure of Example VI was repeated varying the charges as shown in Table IV. (The first entry in Table IV represents the product of Example VI).
  • Example VI utilized half esters which are substantially more hydrophilic than the methacrylate ester of similar hydrophobic chain length and, as such, it is necessary only to adjust the water/cosolvent ratio used during the reaction to within a range of about 1.2 to about 5.3 in order to account for the increased hydrophilic nature of the hydrophobic monomer.
  • the following example illustrates the preparation of a terpolymer of acrylic acid, maleic acid and Methacrylester C13 according to the method of the present invention.
  • an initial charge was made up consisting of deionized water 360g, isopropanol 200g, maleic anhydride 98g, and sodium hydroxide pellets 72g (1.8 moles).
  • the alkali/water mix hydrolyzed in situ the maleic anhydride to form 1 mole of maleic acid neutralized to 90%.
  • the reactor and its contents were then heated to 80-85°C.
  • reaction contents were held at 80-85°C for a further hour, and the isopropanol substantially removed by azeotropic distillation.
  • a mixture of sodium hydroxide, 120g (3 moles) dissolved in 294g deionized water was added to give a product at approximately pH7.
  • the product had a calculated mole ratio (in the acid form) of acrylic acid 3.5: maleic acid 1.0 methacrylic ester 0.076.
  • the polymer was a viscous opaque single phase liquid, solids 41.8%, pH 7.1; viscosity 4800 cps (spindle 2, 10 rpm); Mw 16,500; and Mn 3000, and had an 0.25% turbidity of 72 N.T.U.'s and was stable for a period of at least two weeks.
  • Example VIII The monomer, polymer to aqueous solvent as well as the water to cosolvent ratios for Example VIII and for Examples IX to XIII are presented in Table V.
  • Example VIII The procedure of Example VIII was repeated, except that the cosolvent used was normal propanol instead of isopropanol. All other conditions were identical.
  • the polymer was a viscous opaque phase liquid, solids 41.9%; pH 7.2; viscosity 14,700 cps (spindle 4, 10 rpm); Mw 35,000; Mn 3700, and had an 0.25% turbidity of 67 N.T.U.'s and was stable for a period of at least two weeks.
  • the product had a calculated mole ratio (in the acid form) of acrylic acid 3.0: maleic acid 2.0: methacrylic ester 0.093.
  • the polymer was a viscous opaque single phase liquid, solids 47.4%, viscosity 4000 cps (spindle 4, speed 20 rpm); Mw 9800 and Mn 2000, and had an 0.25% turbidity of 46 N.T.U.'s and was stable for a period of two weeks.
  • the product had a calculated mole ratio (in the acid form) of acrylic acid 3.0: maleic acid 2.0: methacrylic ester 0.197.
  • the product was a viscous, opaque single phase liquid, solids 49.4%, viscosity 3500 cps (spindle 4, speed 20 rpm); Mw 5700; Mn 1500, and pH 7.5, an 0.25% turbidity of 120 N.T.U.'s and was stable for a period of at least two weeks.
  • Example XI Another polymer was prepared using the procedure and materials of Example XI but changing the water content to 250 g and the isopropanol to 250 g.
  • the resulting product was a homogeneous, viscous, semi-opaque single phase liquid with solids 43.4%, viscosity 1320 (spindle 3, speed 20) Mw 6200, Mn 1400 and pH 8.1, 0.25% turbidity of 18 N.T.U.'s and was stable for a period of at least two weeks.
  • Example IX and X were repeated reducing the levels of n-propanol and isopropanol in the initial charge to 100 g and 75 g, respectively.
  • the procedure of Example XI was also repeated varying the amount of water to 225 g and the isopropanol to 400 g in the initial charge.
  • an acrylate, maleate, methacrylester C13 terpolymer can be prepared with Mw of 5000 to 40,000 at a conveniently usable solids and viscosity relationship using a water to cosolvent ratio of about 1.0 to 3.6 during the reaction, and obtaining an opaque or semi-opaque product with an 0.25% turbidity greater than 10 N.T.U.'s which is stable for at least two weeks.
  • the following example illustrates the production of copolymers of acrylic acid and vinyl esters.
  • Example I The procedure of Example I was essentially repeated to prepare two polymers (XIVA and XIVB) using acrylic acid and vinyl laurate in a mole ratio of 25:1.
  • copolymer XIVB was prepared using normal propanol and an initiator of 100 g of 1% sodium persulphate, with final neutralization to pH 4 using approximately 0.28 moles of 10% sodium hydroxide.
  • copolymers XIVC and XIVD were prepared from a 25:1 ratio of acrylic acid to VeoVa®, a vinyl ester of Versatic 10® (a C10 isomeric mixture of synthetic saturated mono-carboxylic acid) available from Shell.
  • Example I The procedure of Example I was essentially repeated to prepare 3 polymers (XV A-C) using acrylic acid and the surfactant type methacrylate in a mole ratio of 25:1.
  • the cosolvent was isopropanol, the initiator 80 g of a 5% solution of sodium persulphate, and neutralization with 230 g of 48% sodium hydroxide solution.
  • the cosolvent/monomer ratio was 2.3 and the cosolvent/polymer ratio was 2.6.
  • Table VII The properties of these polymers are presented in Table VII.
  • An opaque copolymer is obtained (XV A) at a low viscosity, high solids with a 0.25% turbidity of greater than 10 NTU's, and this was stable for a period in excess of 2 weeks, using a water/cosolvent ratio of 5.0-5.8 during the reaction.
  • a very high viscosity, low solids product (XV, B,C) is obtained where the 0.25% turbidity is less than 10 N.T.U.'s.
  • DMDAAC dimethyl diallyl ammonium chloride
  • Methacrylester 13 The following example illustrates the production of copolymers of dimethyl diallyl ammonium chloride (DMDAAC) and Methacrylester 13.
  • Example II To the reaction vessel set up as in Example I was added an initial charge of 25 g deionized water, 25 g (0.098 moles) Methacrylester 13, 188 g of a 60% aqueous solution of DMDAAC (0.70 moles), 0.5 g ethylene diamine tetra acetic acid, tetra sodium salt (EDTA) and 50 g of isopropanol as the cosolvent.
  • the polymer prepared as Example XIV A had a solids content of 47.9%, a viscosity of 250 cps, a SV of 5.3, pH 1.7, was opaque with a 0.25% turbidity of 215 N.T.U.'s, and was stable for a period of at least 2 weeks.
  • Example XVI A Using the same prodcedure as Example XVI A, 6 additional polymers (XVI B-G) were prepared in order to determine the precise final water/cosolvent ratios useful in the preparation of this specific copolymer. The water/cosolvent amounts were varied as noted in Table VIII.
  • Stable opaque products were produced (XVI A-D) with a 0.25% turbidity of greater than 10 N.T.U.'s, which were stable for a period of at least 2 weeks with convenient high solids and low viscosities, when a final water/isopropanol ratio was approximately in the range 1.6-7.0.
  • Example XVI The following example illustrates the production of DMDAAC Methacrylester 13 copolymers, using a slightly different procedure to that of Example XVI, and covering different standard viscosities (S.V.'s), and mole ratios.
  • the initial charge was deionized water 50 g, EDTA 0.5g, DMDAAC (60% aqueous) 125 g (0.46 moles).
  • Three independent streams of reactants were pumped in, keeping the reaction mass at 80-85°C., being DMDAAC (60% aqueous) 500g (1.86 moles) over 3 hours; a mixture of isopropanol as cosolvent, 50 g and Methacrylester 13, 25 g (0.094 moles) over 3 hours, and 100 g of 8% solution aqueous solution of sodium persulphate over 4 hours.
  • the reactor contents were held at 80-85°C for a period of a further hour.
  • the ratio of hydrophilic to hydrophobic monomer was 25:1 molar, and the ratio of water (from all sources) to cosolvent was 8.0:1 at the end of the reaction.
  • Polymer work up was similar to Example XVI A.
  • the polymer prepared as Example XVII A had a solids content of 43.6%, a viscosity of 620 cps, a S.V. of 12.9, pH 1.1, and was semi-opaque with a 0.25% turbidity of 12.5 N.T.U.'s, and was stable for a period of at least 2 weeks.
  • Example XVII B-D 3 additional polymers (XVII B-D) were prepared in order to illustrate variation in S.V., and mole ratios of hydrophilic to hydrophobic monomer.
  • the initial charge, and monomer addition remained identical to Example XVII A. Variations were made in the amount of isopropanol, Methacrylester 13 and sodium persulphate used, and are noted in Table IX.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymerisation Methods In General (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Graft Or Block Polymers (AREA)
EP89110694A 1988-06-13 1989-06-13 Procédé de préparation de polymères Expired - Lifetime EP0346834B1 (fr)

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GB888813966A GB8813966D0 (en) 1988-06-13 1988-06-13 Process for manufacture of polymers
GB8813966 1988-06-13

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EP0346834A2 true EP0346834A2 (fr) 1989-12-20
EP0346834A3 EP0346834A3 (fr) 1991-05-29
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EP (1) EP0346834B1 (fr)
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DE (1) DE68920779T2 (fr)
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US6177396B1 (en) 1993-05-07 2001-01-23 Albright & Wilson Uk Limited Aqueous based surfactant compositions

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US6199318B1 (en) 1996-12-12 2001-03-13 Landec Corporation Aqueous emulsions of crystalline polymers for coating seeds
US9259598B2 (en) * 1996-12-12 2016-02-16 Landec, Inc. Aqueous dispersions of crystalline polymers and uses
US6540984B2 (en) * 1996-12-12 2003-04-01 Landec Corporation Aqueous dispersions of crystalline polymers and uses
US6239240B1 (en) * 1997-01-28 2001-05-29 Stepan Company Emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids
ATE258561T1 (de) * 1997-01-28 2004-02-15 Stepan Co Emulsionspolymerisationsverfahren unter verwendung von ethylenisch ungesättigten aminsalzen von sulfonsäure,phosphorsäure und carbonsäure
US7423167B2 (en) * 1997-01-28 2008-09-09 Stepan Company Ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids
US20020161108A1 (en) * 2000-03-09 2002-10-31 Stepan Company, A Corporation Of The State Of Delaware Emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids
US5979131A (en) * 1998-04-15 1999-11-09 Sto Corp. Exterior insulation and finish system
US7101928B1 (en) * 1999-09-17 2006-09-05 Landec Corporation Polymeric thickeners for oil-containing compositions
WO2002062861A1 (fr) * 2001-01-05 2002-08-15 The Ohio State University Research Foundation Nouveaux polymeres solubles dans l'eau contenant des residus d'amide cyclique ou d'amide vinylique, destines a des produits de restauration dentaire
JP3999746B2 (ja) * 2003-05-19 2007-10-31 ローム アンド ハース カンパニー ポリマーナノ粒子の高固形分調製方法
US7504466B2 (en) * 2004-11-04 2009-03-17 Rohm And Haas Company High solids preparation of crosslinked polymer particles
JP5221958B2 (ja) * 2005-11-14 2013-06-26 住友精化株式会社 アルキル変性カルボキシル基含有水溶性共重合体
EP1953176B1 (fr) * 2005-11-21 2011-07-06 Sumitomo Seika Chemicals Co., Ltd. Copolymere hydrosoluble ayant un groupe carboxyle modifie par un alkyle
JP5109464B2 (ja) * 2007-04-27 2012-12-26 東亞合成株式会社 （メタ）アクリル酸塩系重合体の製造方法
US8814950B2 (en) 2008-11-17 2014-08-26 The Trustees Of Columbia University In The City Of New York Detergent compositions utilizing hydrophobically modified polymer
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US6177396B1 (en) 1993-05-07 2001-01-23 Albright & Wilson Uk Limited Aqueous based surfactant compositions

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ATE117698T1 (de) 1995-02-15
JPH0270705A (ja) 1990-03-09
CA1338483C (fr) 1996-07-23
GB8813966D0 (en) 1988-07-20
JP2975379B2 (ja) 1999-11-10
DE68920779T2 (de) 1995-05-18
EP0346834A3 (fr) 1991-05-29
EP0346834B1 (fr) 1995-01-25
US5021525A (en) 1991-06-04
DE68920779D1 (de) 1995-03-09
ES2068218T3 (es) 1995-04-16
GR3015546T3 (en) 1995-06-30

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